Home NDC 61333-500 BZK Antiseptic
Product NDC 61333-500
11-digit product format 613330500
Labeler code 61333
Product ID 61333-500_48efec8f-83e6-0744-e063-6394a90a0c29
Type HUMAN OTC DRUG
Nonproprietary name benzalkonium chloride
Dosage form SWAB
Route TOPICAL
Labeler Lights Medical Manufacture Co., Ltd.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-06-02
Substance BENZALKONIUM CHLORIDE
Active strength .13 mg/100mg
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 61333-500-01 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 61333-500-01 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base BZK Antiseptic
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .13 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1038558 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61333-500-01 BZK Antiseptic 1 in 1 PACKAGE SWAB 1 9 61333-500-01 BZK Antiseptic 0.4 mg in 1 POUCH SWAB 0.4 9
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61333-500 BZK ANTISEPTIC (BENZALKONIUM CHLORIDE) SWAB [LIGHTS MEDICAL MANUFACTURE CO., LTD.] 8 Current NDC, Legacy NDC, 2 package rows 20241226_698ed472-9204-46e3-95a4-d59e204628ac.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 8 of 49 · 973 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 61333-500-01 61333050001 1 POUCH in 1 PACKAGE (61333-500-01) / .4 mg in 1 POUCH 1 pouch 2021-06-02 0000-00-00 No No Current